R&D Engineer- Medical Device #9881

About ECI ECI's mission is to be the global leader of professional consulting services for the life sciences industry.

Our clients lean on our diverse perspectives and decades of expertise to tackle their toughest challenges, and we take pride in providing them transformative solutions with distinctive, sustainable and long-term value.

ECI boasts a proven track record of providing full product life cycle consulting on a variety of challenging and exciting projects.

Our collaborative culture, welcoming team and flexible employment & benefit options allow us to maintain strong relationships with the most talented individuals in the life sciences industry.About the Role As a R&D Engineer- you will lead and support design control related activities for the class II and III medical devices and combination products.

The successful candidate will support design history file remediation project with design control related expertise as part of the project team.

The position offers opportunities to work in multidisciplinary teams, across projects, where specific contribution within quality systems is a key element for success.

What You will Do: Review of Design History Files (DHF) and/or associated documentation for compliance gaps to regulations, standards and/or the company's quality management system requirements.

Document a comprehensive gap assessment report summarizing applicable regulatory and/or standards deficiencies Develop a summary of recommendations for successful remediation of the DHF Execute remediation of each DHF file based on the gaps identified: Leads and successfully contributes to DHF remediation project teams typically including the following activities: design and development plan, design reviews, design input, design output, Risk management, usability studies, design verification and validation, test method development and validation, research investigations, report preparation, and process/test documentation ensuring compliance to design control requirements Support product specifications development, including engineering/technical protocols and reports Update/develop all associated documentation related to DHFs.

This may include all elements of design control.

Coordinate documentation activities with other functional groups including research and development, design quality assurance, regulatory compliance, clinical affairs, and marketing Develop risk management deliverables in compliance with ISO 14971 Develop usability documentation in compliance with ISO 62366 Develop, execute and summarize System DVMP, design verification and validation protocols and reports Develop and validate test methods Compile, summarize, and analyze test results Develop retrospective analysis to support the continued marketing of the devices Ensure that all required technical documentation for medical devices comply with company and regulatory requirements.

Support and participate in key project meetings, e.g.

Design reviews Lead effectively within...